

This site is not affiliated, endorsed or administered by the Food and Drug Administration (FDA). Reliance on any information provided by the National Drug Codes List website or other visitors to this website is solely at your own risk. The contents of the National Drug Codes List website are provided for educational purposes only and are not intended in any way as medical advice, medical diagnosis or treatment. NDC List 2022 | NDC Data Last Updated: 07-01-2022Īll contents of this website are provided on an "as is" and "as available" basis without warranty of any kind. Inactive ingredients ethyl alcohol (SDA 40B), propylene glycol, purified water

Stop use and ask a doctor ifthis product, used as directed, does not provide relief.When using this product avoid contact with the eyes. UseHelps in temporarily prolonging time until ejaculation Values = "Y", "N", "E", or "I".ĭistributed by Roman Health Ventures, Inc.29 W 30th St. This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). This is the date when the listing record will expire if not updated or certified by the product labeler.Įxclude Flag: N - NO What is the NDC Exclude Flag? Listing Expiration Date: 12-31-2023 What is the Listing Expiration Date? This is the date that the labeler indicates was the start of its marketing of the drug product. Start Marketing Date: 01-10-2019 What is the Start Marketing Date?

The complete list of codes and translations can be found at under Structured Product Labeling Resources. Currently, only final marketed product categories are included. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. Marketing Category: OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph. For unapproved drugs, this field will be null. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated.
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Name of Company corresponding to the labeler code segment of the Product NDC.įDA Application Number: part348 What is the FDA Application Number? Product Labeler Information What is the Labeler Name?
